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- Title:
Changes in adiponectin multimer distribution in response to atorvastatin treatment in patients with type 2 diabetes.
- Document type:
- Journal Article
- Author(s):
- von Eynatten, M; Liu, D; Bluemm, A; Schuster, T; Baumann, M; Lutz, J; Heemann, U; Dugi, K; Nawroth, P; Bierhaus, A; Humpert, P
- Abstract:
- OBJECTIVE: Multimeric high molecular weight (HMW) forms of adiponectin were previously shown to be inversely associated with the extent of atherosclerosis in males and are down-regulated in patients with the metabolic syndrome and type 2 diabetes. In this study, potential influences of atorvastatin therapy on adiponectin multimer distribution were studied in patients with type 2 diabetes. DESIGN, PATIENTS AND MEASUREMENTS: The effect of 40 mg atorvastatin on HMW, medium molecular weight (MMW), and low molecular weight (LMW) isoforms of adiponectin were investigated in 75 patients (23 females; 52 males) with type 2 diabetes in an 8-week-long, placebo-controlled and randomized study. Adiponectin multimeric isoforms were detected by Western blot analysis. RESULTS: After atorvastatin therapy the median serum concentration of HMW adiponectin increased significantly by 42.3% (1.68 vs. 2.39 microg/ml; P < 0.001), while concentrations of MMW adiponectin and LMW adiponectin significantly decreased by 20.8% and 23.2%, respectively (MMW: 3.31 vs. 2.62 microg/ml, P = 0.047; LMW: 0.56 vs. 0.43 microg/ml, P = 0.033). Median total adiponectin levels were not significantly altered by atorvastatin treatment (6.0 vs. 6.2 microg/ml, P = 0.898). Consequently, the HMW: total-adiponectin ratio significantly increased by 25.0% (0.40 vs. 0.50; P = 0.013). CONCLUSIONS: Atorvastatin therapy is associated with significant changes in adiponectin multimer distribution in patients with type 2 diabetes. Since total adiponectin levels were not affected by intervention, atorvastatin may shift adiponectin size towards the HMW form.
- Journal title abbreviation:
- Clin Endocrinol (Oxf)
- Year:
- 2009
- Journal volume:
- 71
- Journal issue:
- 1
- Pages contribution:
- 27-32
- Language:
- eng
- Fulltext / DOI:
- doi:10.1111/j.1365-2265.2008.03412.x
- Pubmed ID:
- http://view.ncbi.nlm.nih.gov/pubmed/18778396
- Print-ISSN:
- 0300-0664
- TUM Institution:
- Institut für Medizinische Statistik und Epidemiologie
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